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Michael H. Weisman - Ankylosing Spondylitis

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Ankylosing Spondylitis is an inflammatory arthritis that affects the spine and sacroiliac joints as well as other parts of the body, and that can eventually lead, in some patients, to complete fusion of the vertebrae and total rigidity. AS is not a rare health problem, but is in fact found in almost one percent of the US population, typically strikes young people and young families, and in its various forms is probably more common than rheumatoid arthritis. In this invaluable guide, Dr. Michael H. Weisman, one of Americas leading authorities on AS, provides a down-to-earth, crystal-clear guide that is ideal for patients and their family. Dr. Weisman explains what AS is, discusses the genetic background to the disease (including the genes that researchers think may predispose some people to AS), explains how to diagnose the disease early and possibly prevent the later development of debilitating rigidity, the use of MRI for early detection, and much more. The book outlines which medications (such as TNF inhibitors) seem the most promising right now, the various drug side effects, the value of physical therapy, other treatment approaches, and whether surgery can be used to manage the complications of the disease. AS can lead to severe disability, but even those who have a milder form will experience painful flares alternating with periods of remission. Since it is a progressive disease in many patients, it is very important to reach patients as early as possible. This book will arm patients with the vital information they need to combat the disease. Laurie M. Savage, the Executive Director of the Spondylitis Association of America (SSA), the main patient support group world-wide, has written a foreword to the book. In addition, SSA will endorse the book and their logo will appear on the cover.

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ANKYLOSING SPONDYLITIS
Ankylosing Spondylitis

MICHAEL H. WEISMAN, MD

Ankylosing Spondylitis - image 1

Ankylosing Spondylitis - image 2

Oxford University Press, Inc., publishes works that further Oxford University's
objective of excellence in research, scholarship, and education.

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Copyright 2011 by Oxford University Press, Inc.

Published by Oxford University Press, Inc.
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All rights reserved. No part of this publication may be reproduced, stored in a
retrieval system, or transmitted, in any form or by any means, electronic, mechanical,
photocopying, recording, or otherwise, without the prior permission
of Oxford University Press.


Library of Congress Cataloging-in-Publication Data
Weisman, Michael H.
Ankylosing spondylitis / Michael H. Weisman. p. ; cm.
Includes bibliographical references and index. ISBN 978-0-19-539910-3
1. Ankylosing spondylitisPopular works. I. Title.
[DNLM: 1. Spondylitis, AnkylosingPopular Works. WE 725]
RD771.A5W45 2011
616.7'3dc22 2010041913


9 8 7 6 5 4 3 2 1
Printed in USA
on acid-free paper

CONTENTS

PART TWO WHERE AND HOW THE
BODY CAN BE AFFECTED BY
ANKYLOSING SPONDYLITIS

ANKYLOSING SPONDYLITIS
PART ONE

INTRODUCTION
AND OVERVIEW

THE FIRST CHAPTER in this section,


Overview of Ankylosing
Spondylitis

ANKYLOSING SPONDYLITIS (AS) is one of several conditions that belong to a group of chronic inflammatory rheumatic disorders known as spondyloarthropathies (SPAs). It is a chronic systemic inflammatory disease that primarily attacks the axial skeleton and adjacent structures. The axial skeleton () consists of 80 bones in the head and trunk of the body, and is divided into five parts: skull, ossicles of the inner ear, hyoid bone of the throat, rib cage, and the vertebral column.

Typically, the vertebrae of the spine become inflamed, causing chronic pain and discomfort. In more severe cases, this inflammation can lead to new bone formation on the spine, causing the spine to fuse in a fixed, immobile position resulting in a forward-stooped posture. If left untreated, the inflammation of the spinal joints will gradually destroy the cartilage and fibrous tissue of the surrounding structures as well as the ligaments and literally replace them with bone. There appears to be a cyclical process to the disease (). Interrupting this cycle with early identification of the disease and aggressive treatment may prevent the immobility and stooped posture caused by spinal fusion.

The effects of AS are not confined to the spine. Patients with AS may experience pain and inflammation in other joints, such as hips, shoulders, knees, elbows, and feet. Ankylosing spondylitis may also affect the lungs, eyes, bowel and, in rare cases, the heart. There is a considerable genetic and clinical overlap between AS and inflammatory bowel disease, the causes of which are being investigated. Details of the effects of AS on other parts of the body, and the signs, symptoms, and treatment of conditions associated with AS will be discussed in later chapters.

FIGURE 11 Axial Spine FIGURE 12 AS Inflammatory Disease Process - photo 3

FIGURE 1.1 Axial Spine

FIGURE 12 AS Inflammatory Disease Process CLASSIFICATION CRITERIA The - photo 4

FIGURE 1.2 AS Inflammatory Disease Process

CLASSIFICATION CRITERIA

The diagnosis of AS is based on clinical features and radiographic (X-ray) criteria. Unfortunately, there are no laboratory tests that can be used to establish a diagnosis of AS with certainty. The modified New York 1984 criteria () are the most commonly used criteria to classify AS. Diagnostic criteria for AS have been recommended, but have not been validated through scientific study.

Classification criteria for AS, and other rheumatic diseases such as rheumatoid arthritis, are used to identify patients for research and genetic studies. To be useful for research, treatment protocols, and genetic studies, it is important that the classification criteria correctly and definitively identify patients with the disease. This means that the usual classification criteria identify patients with a disease that is recognizable and quite certainly established with little doubt. Because classification criteria almost always require changes in the body that indicate that the disease has been present for some time, it is difficult to develop diagnostic criteria ahead of permanent damage. In the case of AS, classification criteria require X-ray evidence of damage to the spine. However, we want to diagnose AS patients before spinal damage has occurred; therefore, any diagnostic criteria need to be based on a probability that the patient has AS. This is the challenge that physicians face today in diagnosing ASto develop diagnostic criteria that we can apply earlier in the course of disease and before damage has occurred to the spine. In other words, we want to diagnose patients with AS before or ahead of the time they fulfill classification criteria.

Table 1.1


MODIFIED NEW YORK CLASSIFICATION CRITERIA
FOR ANKYLOSING SPONDYLITIS


Clinical Components

Low back pain and stiffness for 3 months that improves with exercise but not with rest

Limitation of lumbar spine mobility in both the sagittal (sideways) and frontal (forward and back) planes

Limitation in chest expansion as compared with normal range for age and gender

Radiologic Component

Unilateral sacroiliitis of Grade 3 or 4, or bilateral sacroiliitis of Grade 2

Diagnosis

Definite AS if the radiological criterion is associated with at least one clinical component

Probable AS if:

Only the three clinical components are present or

Only the radiologic component is present


Fortunately, new classification criteria recently developed and refined by the Assessment of SpondyloArthritis international Society (ASAS) provide guidelines to aid in the diagnosis of patients prior to the appearance of positive radiographic findings.


History of Ankylosing
Spondylitis

THE WORDS ankylosing and spondylitis are of Greek origin. Angylos means bent or crooked, and refers to the stooped or bent posture that may occur in AS patients. Spondylos means spinal vertebrae, and itis means inflammation. Spondylitis, then, is an inflammation of the vertebrae. The historical dating of ankylosing spondylitis (AS) is controversial and remains the subject of considerable debate, with some investigators dating the first incidence of AS to antiquity, while others contend that AS is of more recent origin. Based on paleopathologic studiesthe study of diseases in ancient remains or medical writingsa number of researchers have concluded that evidence from humans and animals indicates that the origins of AS go as far back as several thousand years BC. For example, Egyptian pharaohs, including Amenhotep II (reign 14271401 BC), Ramses the Great (reign 12791213 BC), and Ramses son Merneptah (reign 12131203 BC), have been described as having AS. During the fifth century, Hippocrates, author of the Hippocratic oath by which all physicians are bound to ethically practice medicine, described a condition suggestive of AS. Other researchers have determined that ancient cases of AS are more likely cases of a condition known as

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